rs2279008
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2279008(A;A) |
| Make rs2279008(A;G) |
| Make rs2279008(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 17172493 |
| Gene | MYO9B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2279008 |
| dbSNP (classic) | rs2279008 |
| ClinGen | rs2279008 |
| ebi | rs2279008 |
| HLI | rs2279008 |
| Exac | rs2279008 |
| Gnomad | rs2279008 |
| Varsome | rs2279008 |
| LitVar | rs2279008 |
| Map | rs2279008 |
| PheGenI | rs2279008 |
| Biobank | rs2279008 |
| 1000 genomes | rs2279008 |
| hgdp | rs2279008 |
| ensembl | rs2279008 |
| geneview | rs2279008 |
| scholar | rs2279008 |
| rs2279008 | |
| pharmgkb | rs2279008 |
| gwascentral | rs2279008 |
| openSNP | rs2279008 |
| 23andMe | rs2279008 |
| SNPshot | rs2279008 |
| SNPdbe | rs2279008 |
| MSV3d | rs2279008 |
| GWAS Ctlg | rs2279008 |
| GMAF | 0.2617 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | Height |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | T |
| P-val | 3E-8 |
| Odds Ratio | .03 [NR] unit increase |
